Detalhe da pesquisa
1.
Development of an oral treatment that rescues gait ataxia and retinal degeneration in a phenotypic mouse model of familial dysautonomia.
Am J Hum Genet
; 110(3): 531-547, 2023 03 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36809767
2.
Selective retinal ganglion cell loss and optic neuropathy in a humanized mouse model of familial dysautonomia.
Hum Mol Genet
; 31(11): 1776-1787, 2022 06 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34908112
3.
Transcriptome analysis in a humanized mouse model of familial dysautonomia reveals tissue-specific gene expression disruption in the peripheral nervous system.
Sci Rep
; 14(1): 570, 2024 01 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-38177237
4.
Transcriptome analysis in a humanized mouse model of familial dysautonomia reveals tissue-specific gene expression disruption in the peripheral nervous system.
bioRxiv
; 2023 Oct 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37808686
5.
16p12.1 Deletion Orthologs are Expressed in Motile Neural Crest Cells and are Important for Regulating Craniofacial Development in Xenopus laevis.
Front Genet
; 13: 833083, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35401697
6.
Author Correction: Transcriptome analysis in a humanized mouse model of familial dysautonomia reveals tissue-specific gene expression disruption in the peripheral nervous system.
Sci Rep
; 14(1): 10103, 2024 May 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38698036